Clinical Trials Assistant Bradford
- Recruiter
- IQVIA CSMS
- Location
- United Kingdom
- Salary
- Competitive
- Posted
- 01 Jul 2022
- Closes
- 09 Jul 2022
- Sectors
- Scientific & Pharmaceutical
- Contract Type
- Permanent
- Hours
- Full Time
Clinical Research Assistant / Clinical Trial Assistant, Bradford
12 - 24h/ week for 12 weeks (with potential additional extension for additional 12 weeks)
Flexible hours to suit you (during working hours, 8am-6pm Monday - Friday)
Are you looking for your next opportunity in Clinical Research? Do you want to work for an industry leading company that offers you an excellent benefits package and supports career progression? If so, come and join us - IQVIA are looking for an experienced site-based Clinical Research Assistant in Bradford.
As a pivotal member of the site team, you will be involved with a variety of administrative tasks to support investigators and ensure the smooth running of clinical trials and assist with collecting patient data.
Day to day responsibilities will include:
Verifying and/or correcting research study information on source documents; researching queries and variances; providing feedback to the site data collector
Accurate input of trial data into the Electronic Data Capture (EDC) system
Preparing / maintaining study files, and submission of information according to deadlines
Collecting / submitting and assisting in maintaining relevant regulatory and ethics documentation
Scheduling visits with research subjects and generating appropriate reports and documentation
Tracking patient visits and procedures completed against the study budget by inputting data into the clinical trial management system (CTMS)
Processing lab specimens including labelling of vials and accurately filling out requisitions for storage and/or shipment per the study protocol and shipment regulations
Performing other administrative support functions such as reception, office organization, and office supply management .
We are looking for candidates with the following skills and experience:
BS/BA in life sciences or educational equivalent and/or relevant work experience in a clinical environment or medical setting, e.g. clinical research coordinator, nurse, medical assistant, other medical profession
Basic knowledge of clinical trials, combined with in-depth knowledge of departmental, protocol and study-specific operating procedures, consent forms, and study schedules
Basic knowledge of medical terminology
Strong IT competence, skilled in using MS Windows and Office applications such as Access, Outlook, Excel, and Word
Excellent interpersonal skills with the ability to establish and maintain effective working relationships with co-workers, managers and clients
Good organisational skills with the ability to pay close attention to detail.
IQVIA is a leading global provider of advanced analytics, technology solutions and clinical research services to the life sciences industry. We believe in pushing the boundaries of human science and data science to make the biggest impact possible - to help our customers create a healthier world. Learn more at
12 - 24h/ week for 12 weeks (with potential additional extension for additional 12 weeks)
Flexible hours to suit you (during working hours, 8am-6pm Monday - Friday)
Are you looking for your next opportunity in Clinical Research? Do you want to work for an industry leading company that offers you an excellent benefits package and supports career progression? If so, come and join us - IQVIA are looking for an experienced site-based Clinical Research Assistant in Bradford.
As a pivotal member of the site team, you will be involved with a variety of administrative tasks to support investigators and ensure the smooth running of clinical trials and assist with collecting patient data.
Day to day responsibilities will include:
Verifying and/or correcting research study information on source documents; researching queries and variances; providing feedback to the site data collector
Accurate input of trial data into the Electronic Data Capture (EDC) system
Preparing / maintaining study files, and submission of information according to deadlines
Collecting / submitting and assisting in maintaining relevant regulatory and ethics documentation
Scheduling visits with research subjects and generating appropriate reports and documentation
Tracking patient visits and procedures completed against the study budget by inputting data into the clinical trial management system (CTMS)
Processing lab specimens including labelling of vials and accurately filling out requisitions for storage and/or shipment per the study protocol and shipment regulations
Performing other administrative support functions such as reception, office organization, and office supply management .
We are looking for candidates with the following skills and experience:
BS/BA in life sciences or educational equivalent and/or relevant work experience in a clinical environment or medical setting, e.g. clinical research coordinator, nurse, medical assistant, other medical profession
Basic knowledge of clinical trials, combined with in-depth knowledge of departmental, protocol and study-specific operating procedures, consent forms, and study schedules
Basic knowledge of medical terminology
Strong IT competence, skilled in using MS Windows and Office applications such as Access, Outlook, Excel, and Word
Excellent interpersonal skills with the ability to establish and maintain effective working relationships with co-workers, managers and clients
Good organisational skills with the ability to pay close attention to detail.
IQVIA is a leading global provider of advanced analytics, technology solutions and clinical research services to the life sciences industry. We believe in pushing the boundaries of human science and data science to make the biggest impact possible - to help our customers create a healthier world. Learn more at